Hand Sanitizer
FDA Label NDC 47993-278

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Hand Sanitizer (NDC 47993-278). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - when using, otc - stop use, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredients

Ethyl Alcohol 70%

Otc - Purpose

Antiseptic

Indications & Usage

Uses：

For hand sanitizing to reduce bacteria on the skin.

Warnings

Warnings:

  • Flammable. 
  • Keep away from fire or flame.
  • For external use only.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Otc - When Using

  • Keep away from eyes.
  • Do not inhale or ingest.

Otc - Stop Use

  • Stop use and ask a doctor if irritation or redness develops.

Dosage & Administration

Directions:

  • Squeeze small amount in your palm and briskly rub hands together, and allow to air dry.
  • For children under 6, use with adult supervision. Not recommended for infants.

Other Safety Information

Other information：

  • Store below 110℉(43℃)
  • May discolor certain fabrics or surfaces.

Inactive Ingredient

Inactive Ingredients:

Water,Carbomer 940,triethanolamine,Glycerin,Aloe Barbadensis

Package Label.Principal Display Panel

Image Of Hand Sanitizer 237ml (237ml)

Image Of Hand Sanitizer 237ml (237ml)

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